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Here goes nothing .... MRI in 45 minutes


Carey
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I DESPISE getting MRIs of the head.  Claustrophobia is bad enough without putting your head in a vise too, but I go for an update to see where I stand with the alien invasion in my head. I'm really hoping theres been some significant change for the good.  meds to counteract side effects of meds on top of other meds ... well it's getting old and I'm worn down about as far as I can go. I have no energy, taste buds are fried, vision has been affected, balance .... etc.  Tired of feeling like an invalid and would like to see a benefit to all this torture.  That's what I want most this Christmas.  Wish me luck.

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Carey,

  So you had to have a brain MRI?

I know those suck, ice had several & my future says I'll have many more.

 

  What where they checking for?

 

I have Chiari 1 Malformation (brain herniation) & know to much on that subject.

 

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I hope your results showed improvement, Carey! You deserve some good news!

 

Torn, my son had brain surgery a few years ago for his Chiari Malformation. It was very scary to go through, but it was successful and even allowed for his scoliosis to improve some. I'm sorry you are dealing with the Chiari.

 

Hugs to you both!

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I hope your results showed improvement, Carey! You deserve some good news!

 

Torn, my son had brain surgery a few years ago for his Chiari Malformation. It was very scary to go through, but it was successful and even allowed for his scoliosis to improve some. I'm sorry you are dealing with the Chiari.

 

Hugs to you both!

 

Thanks for the encouragement,it's my goal in life to see a specialist,I await insurance that will allow me to go out of state.

  I'm glad your son us doing better,always a blessing

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Carey,

  So you had to have a brain MRI?

I know those suck, ice had several & my future says I'll have many more.

 

  What where they checking for?

 

I have Chiari 1 Malformation (brain herniation) & know to much on that subject.

 

 

I have an inoperable meningioma.  I've been taking chemo drugs since June to reduce it since I'm not a candidate for surgery.  Chemo is a relatively new thing for meningioma treatment and at first they told me two months, it's been six.  I've had an MRI every 2 months since then and I HATE them.  I used to work for my neurologist and we are actually friends so he usually calls me the same day with the results but I didn't hear from him yesterday so I'm a little worried. The test also took longer than normal too.  If they tell me it's not shrunk any I just don't know what i'll do.  It's not cancerous, but nonetheless it's location is dangerous.

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Well.  It HAS shrunk about a centimeter.  So no, no end to the treatment right now, which is upsetting. I cried for an hour.  Because it's smaller it was able to move and is affecting different areas now, causing nocturnal seizures and hearing problems and balance issues.  I asked when I could reasonably expect to quit the pills and he said no set time just check again in 2 months.  Yet again.  :(

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I'm sorry to hear that there wasn't a more significant change and that you have to continue treatment. I hope the New Year brings you some peace and better health, I think you've more than met your limit of life stresses and deserve a break.

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My heart goes out to you,as I do know the abnormal and dangers if excess pressure in the brain.

  Obviously we all want you 100% better and hopefully you get there soon.

  Like all things,stay positive my sister in head pain,I hope your next scan reveals more marked improvement

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